A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5476450



Internal ID254061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:109146273..109146431hg38UCSC Ensembl
chr8:110158502..110158660hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38159
hg19159
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17015190
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5476450
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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